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Tooth resin treatment soothes sensitive teeth in children

NCT ID NCT07118111

Symptom relief Sponsor: Gizem Tıraşçı Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study tested a resin coating on the front teeth of 40 children aged 7-14 who had weak enamel (hypomineralization or hypoplasia) and tooth sensitivity. The treatment aimed to reduce pain from cold air and improve how kids and parents felt about the look and function of their teeth. Researchers measured sensitivity and satisfaction before treatment and at 1, 3, and 6 months after.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

40 people

The number who actually took part.

Started

Mar 2025

Finished

Jan 2026

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

7 to 14 years

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Children aged between 7 and 14 years. * Children in good general health without any systemic disease. * Presence of at least one anterior permanent tooth with hypomineralization or hypoplasia. * Teeth with lesions larger than 1 mm that are suitable for resin infiltration treatment. * Voluntary participation of both the child and their parent/guardian in the study, with signed informed consent. Exclusion Criteria: * Children with systemic diseases or undergoing medical treatment. * Cases with active caries, trauma, restorations, or endodontic treatment applied or required on anterior teeth. * Individuals who have previously received resin infiltration or similar treatment on the same tooth. * Children with a history of allergies or sensitivity to the materials used in the procedure. * Individuals who have received interventions such as fluoride varnish, fissure sealants, or tooth whitening on their teeth. * Children who do not possess the cognitive ability to understand and respond to the questionnaire or sensitivity assessment.

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Conditions

The condition(s) this trial relates to.

dental enamel hypoplasia dentin sensitivity Molar Hypomineralization

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Dental hypersensitivity Enamel hypoplasia Molar incisor hypomineralisation

Contacts and locations

Locations

  • Inonu University

    Malatya, Battalgazi, 44050, Turkey (Türkiye)

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